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LeritineDrug - Leritine The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Anileridine Phosphate
Strength -
25MG/ML
Applicant -
MERCK
New Drug Application (NDA) Number -
010520
Product Number -
003
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Merck And Co Inc
Leritine
Anagrelide Hcl Eq 1mg Base Capsule; Oral
Anagrelide Hcl Eq 0.5mg Base Capsule; Oral Anagrelide Hcl Eq 1mg Base Capsule; Oral Anagrelide Hcl Eq 0.5mg Base Capsule; Oral Anagrelide Hcl Eq 1mg Base Capsule; Oral Arimidex 1mg Tablet; Oral Leritine Eq 25mg Base Tablet; Oral Leritine 25mg/ml Injectable; Injection Anagrelide Hcl Eq 1mg Base Capsule; Oral Anagrelide Hcl Eq 0.5mg Base Capsule; Oral NewDrugInformation |